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After cleavage reaction, the separation of the 6FAM/Cy5-17DS 6FAM/Cy5-17DS by utilizing fluorescence microscopy (Nikon).

The interparticle fusion and the flow of polymer chains under pressure were monitored by utilizing a non-radiative energy transfer (NRET) method.

The structure and phase of the Group Ti were monitored by utilizing a Philips PW 3710 grazing incidence X-ray diffractometer with a CuK α radiation (scan range 20° to 80°).

The structure and phase of the Group AR were monitored by utilizing a Panalytical diffractometer (Phillips, Holland) using X-ray dataracollecteda collected in the reflection Bragg-Brentano geometry with a CuK α radiation under an applied voltage of 45 kV and a current of 40 mA.

We monitored tumour regression by utilizing fluorescence scanning over the course of cisplatin treatment (Fig 1A).

Intestinal function can be monitored in zebrafish by utilizing microgavage and fluorescent beads or by liposome incubation (Carten et al., 2011; Cocchiaro and Rawls, 2013).

Since proliferating A549 cells did not express CEACAMs, the transfection success could be monitored by flow cytometry utilizing exponentially growing A549 transfectants.

Protein concentration was monitored by the method of Bradford utilizing bovine serum albumin (BSA) as a standard [39].

Changes in the cellular morphology during different growth stages were monitored by standard phase contrast microscopy utilizing the Leica DMIL-system (Leica Microsystems, Wetzlar, Germany) and the ProgRes Capture Pro2.5 analyses software (Jenoptik, Jena, Germany).

Real-time monitoring was possible by utilizing a DNA-specific fluorescent dye and introducing a denaturation step for the paired oligonucleotides, at the highest possible temperature, where the LCR amplicons remained as heterodimers.

Therefore, we could monitor the trypsin activity by utilizing the different fluoresence responses of NAC-CdTe QDs to hemoglobin and hemin.